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Journal Abstract Search

128 related items for PubMed ID: 8041773

  • 1. Structural analysis of chromosomal rearrangements associated with the developmental mutations Ph, W19H, and Rw on mouse chromosome 5.
    Nagle DL, Martin-DeLeon P, Hough RB, Bućan M.
    Proc Natl Acad Sci U S A; 1994 Jul 19; 91(15):7237-41. PubMed ID: 8041773
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  • 2. Lethality of Rw/Rw mouse embryos during early postimplantation development.
    Bućan M, Nagle DL, Hough RB, Chapman VM, Lo CW.
    Dev Biol; 1995 Apr 19; 168(2):307-18. PubMed ID: 7537231
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  • 4. A 1.8-Mb YAC contig spanning three members of the receptor tyrosine kinase gene family (Pdgfra, Kit, and Flk1) on mouse chromosome 5.
    Brunkow ME, Nagle DL, Bernstein A, Bucan M.
    Genomics; 1995 Jan 20; 25(2):421-32. PubMed ID: 7540588
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  • 7. The Wsh and Ph mutations affect the c-kit expression profile: c-kit misexpression in embryogenesis impairs melanogenesis in Wsh and Ph mutant mice.
    Duttlinger R, Manova K, Berrozpe G, Chu TY, DeLeon V, Timokhina I, Chaganti RS, Zelenetz AD, Bachvarova RF, Besmer P.
    Proc Natl Acad Sci U S A; 1995 Apr 25; 92(9):3754-8. PubMed ID: 7537375
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  • 11. Genetic analysis of the dominant white-spotting (W) region on mouse chromosome 5: identification of cloned DNA markers near W.
    Geissler EN, Cheng SV, Gusella JF, Housman DE.
    Proc Natl Acad Sci U S A; 1988 Dec 25; 85(24):9635-9. PubMed ID: 3200849
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  • 12. The mouse Clock mutation behaves as an antimorph and maps within the W19H deletion, distal of Kit.
    King DP, Vitaterna MH, Chang AM, Dove WF, Pinto LH, Turek FW, Takahashi JS.
    Genetics; 1997 Jul 25; 146(3):1049-60. PubMed ID: 9215907
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  • 13. Molecular genetics of the brown (b)-locus region of mouse chromosome 4. II. Complementation analyses of lethal brown deletions.
    Rinchik EM.
    Genetics; 1994 Jul 25; 137(3):855-65. PubMed ID: 8088529
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  • 14. Platelet-derived growth factor receptor alpha-subunit gene (Pdgfra) is deleted in the mouse patch (Ph) mutation.
    Stephenson DA, Mercola M, Anderson E, Wang CY, Stiles CD, Bowen-Pope DF, Chapman VM.
    Proc Natl Acad Sci U S A; 1991 Jan 01; 88(1):6-10. PubMed ID: 1846043
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  • 16. Random mutagenesis of proximal mouse chromosome 5 uncovers predominantly embryonic lethal mutations.
    Wilson L, Ching YH, Farias M, Hartford SA, Howell G, Shao H, Bucan M, Schimenti JC.
    Genome Res; 2005 Aug 01; 15(8):1095-105. PubMed ID: 16024820
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  • 17. Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development.
    Klebig ML, Kwon BS, Rinchik EM.
    Mamm Genome; 1992 Aug 01; 2(1):51-63. PubMed ID: 1543902
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  • 18. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 01; 56(3):105-52. PubMed ID: 19728970
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  • 19. The gene triplet Rw W Ph controls murine haematopoiesis.
    Loutit JF, Cattanach BM, Lyon MF.
    Br J Haematol; 1985 Jun 01; 60(2):219-32. PubMed ID: 4005179
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  • 20. A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis.
    Rinchik EM, Carpenter DA, Selby PB.
    Proc Natl Acad Sci U S A; 1990 Feb 01; 87(3):896-900. PubMed ID: 2300582
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